EZElisa™人混合谱系激酶结构域样蛋白（MLKL）ELI
SA试剂盒-EZElisa™ Human Mixed Lineage Kinase Domain Like Protein (MLKL) ELISA Kit- 询价
- Biogradetech
- 美国
- A-QEK02075-96wells
- 2025年07月16日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
运输过程中保存：2-8℃
- 保质期：
1年
- 英文名：
EZElisa™ Human Mixed Lineage Kinase Domain Like Protein (MLKL) ELISA Kit
- 库存：
100
- 供应商：
艾美捷科技
EZElisa™人混合谱系激酶结构域样蛋白（MLKL）ELISA试剂盒，EZElisa™ Human Mixed Lineage Kinase Domain Like Protein (MLKL) ELISA Kit，混合谱系激酶结构域样蛋白（MLKL）ELISA试剂盒, Mixed Lineage Kinase Domain Like Protein (MLKL) ELISA Kit
产品名称：EZElisa™ Human Mohawk Homeobox（MKX）ELISA试剂盒-EZElisa™ Human Mixed Lineage Kinase Domain Like Protein (MLKL) ELISA Kit
产品货号：A-QEK02075-96wells
产品规格：96wells
Enzyme Immunoassay for the estimation of Mixed Lineage Kinase Domain Like Protein (MLKL) in serum and plasma, tissue homogenates and other biological fluids.
种属：Human
检测方法：比色法
检测范围：0.312 - 20 ng/ml
该EZElisa™人混合谱系激酶结构域样蛋白（MLKL）ELISA试剂盒ELISA的特点包括：即用即用的操作步骤标准化和高重复性批次之间的一致性准确性和精确性经过七个点的验证，符合金环标准质量ELISA的要求，这是Biogradetech质量的基准标志。EZElisa™ ELISA试剂盒用于评估样品中的特定生物标志物，样品可以是血清
运输过程中保存：2-8℃
点击：EZElisa™ Human Mohawk Homeobox（MKX）ELISA试剂盒-EZElisa™ Human Mixed Lineage Kinase Domain Like Protein (MLKL) ELISA Kit更多Biogradetech产品信息价格，货期，产品说明，百度搜“艾美捷科技”进入官网网站，查看具体产品且快速下单。
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文献和实验LINEAGE ANALYSIS USING RETROVIRAL VECTORS
when choosing a vector for lineage analysis are the reporter gene and the promoter that drives its expression. The reporters that have been used include cytoplasmic lacZ [18], nuclear lacZ [19], human placental alkaline phosphatase (PLAP) [20], and avian gag [21
Introduction of human 14-3-3 proteins
inhibitor of protein kinase C,but the N-terminal domain does not inhibit PKC activity.Site-specific mutagenesis of several regions in the tau isoform of 14-3-3,including the mutation of a putative pseudosubstrate site to a potential substrate sequence
Using Phospho‐Motif Antibodies to Determine Kinase Substrates
. Bain, J., Plater, L., Elliott, M., Shpiro, N., Hastie, C.J., McLauchlan, H., Klevernic, I., Arthur, J.S., Alessi, D.R., and Cohen, P. 2007. The selectivity of protein kinase inhibitors: a further update
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